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Supelco

Atrazine-2-hydroxy

PESTANAL®, analytical standard

Synonym(s):

2-Hydroxyatrazine

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About This Item

Empirical Formula (Hill Notation):
C8H15N5O
CAS Number:
2163-68-0
Molecular Weight:
197.24
Beilstein/REAXYS Number:
5870987
MDL number:
MFCD00078693
UNSPSC Code:
41116107
PubChem Substance ID:
329755427
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCNc1nc(O)nc(NC(C)C)n1

InChI

1S/C8H15N5O/c1-4-9-6-11-7(10-5(2)3)13-8(14)12-6/h5H,4H2,1-3H3,(H3,9,10,11,12,13,14)

InChI key

NFMIMWNQWAWNDW-UHFFFAOYSA-N

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General description

Atrazine-2-hydroxy is a non-herbicidal, primary photoproduct obtained upon hydrolytic dechlorination of atrazine.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK7074
BCCF1584
BCBW6506
BCBR9852V
SZBD269XV

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The Triazine Herbicides (2011)
Anaerobic degradation of atrazine
Boopathy R, et al.
International Biodeterioration & Biodegradation, 119, 626-630 (2017)
Milan Hutta et al.
Journal of separation science, 29(13), 1977-1987 (2006-10-05)
A well established method of direct injection of larger than conventional sample volumes ranging from 0.1 mL to 10 mL in HPLC is the injection valve method in which a loop of tubing is totally or partially filled with sample.
J Mahía et al.
Journal of environmental quality, 36(3), 826-831 (2007-05-09)
Mineralization of atrazine and formation of extractable and non-extractable "bound" residues were followed under laboratory conditions in two contrasting soils (organic C, texture, and atrazine application history) from northern Spain. The soils, a Humic Cambisol (MP) and a Gleyic Cambisol
Soil leaching column chromatographic technique for estimation of leaching behavior of atrazine, deethylatrazine, deisopropylatrazine, and hydroxyatrazine on soil.
F Xu et al.
Bulletin of environmental contamination and toxicology, 63(1), 87-93 (1999-07-29)
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